Enhanced Oral Bioavailability and Biodistribution of Voriconazole through Zein-Pectin-Hyaluronic Acid Nanoparticles

被引:1
|
作者
Fin, Margani Taise [1 ]
Diedrich, Camila [1 ]
Machado, Christiane Schineider [1 ]
da Silva, Letícia Marina [1 ]
Tartari, Ana Paula Santos [1 ]
Zittlau, Isabella Camargo [1 ]
Peczek, Samila Horst [1 ]
Mainardes, Rubiana Mara [1 ,2 ]
机构
[1] Laboratory of Nanostructured Formulations, Universidade Estadual do Centro-Oeste-UNICENTRO, Alameda Élio Antônio Dalla Vecchia, 838, PR, Guarapuava,85040-167, Brazil
[2] Pharmacy Department, Universidade Estadual do Centro-Oeste-UNICENTRO, Alameda Élio Antôniom Dalla Vecchia, 838, PR, Guarapuava,85040-167, Brazil
来源
ACS Applied Materials and Interfaces | 2025年 / 17卷 / 01期
关键词
Body fluids - Controlled drug delivery - Hyaluronic acid - Nanoparticles - Pharmacokinetics;
D O I
10.1021/acsami.4c16326
中图分类号
学科分类号
摘要
Nanotechnology-based drug delivery systems offer a solution to the pharmacokinetic limitations of voriconazole (VRC), including saturable metabolism and low oral bioavailability. This study developed zein/pectin/hyaluronic acid nanoparticles (ZPHA-VRC NPs) to improve VRC’s pharmacokinetics and biodistribution. The nanoparticles had a spherical morphology with an average diameter of 268 nm, a zeta potential of −48.7 mV, and an encapsulation efficiency of 88%. Stability studies confirmed resistance to pH variations and digestive enzymes in simulated gastric and intestinal fluids. The in vitro release profile showed a controlled release, with 8% of the VRC released in 2 h and 16% over 24 h. Pharmacokinetic studies in rats demonstrated a 2.8-fold increase in the maximum plasma concentration and a 3-fold improvement in bioavailability compared to free VRC. Biodistribution analysis revealed enhanced VRC accumulation in key organs. These results suggest that ZPHA-VRC NPs effectively improve VRC’s therapeutic potential for oral administration. © 2024 The Authors. Published by American Chemical Society.
引用
收藏
页码:513 / 523
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